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MetaComp: comprehensive analysis software for comparative meta-omics including comparative metagenomics

BACKGROUND: During the past decade, the development of high throughput nucleic sequencing and mass spectrometry analysis techniques have enabled the characterization of microbial communities through metagenomics, metatranscriptomics, metaproteomics and metabolomics data. To reveal the diversity of m...

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Autores principales: Zhai, Peng, Yang, Longshu, Guo, Xiao, Wang, Zhe, Guo, Jiangtao, Wang, Xiaoqi, Zhu, Huaiqiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5625784/
https://www.ncbi.nlm.nih.gov/pubmed/28969605
http://dx.doi.org/10.1186/s12859-017-1849-8
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author Zhai, Peng
Yang, Longshu
Guo, Xiao
Wang, Zhe
Guo, Jiangtao
Wang, Xiaoqi
Zhu, Huaiqiu
author_facet Zhai, Peng
Yang, Longshu
Guo, Xiao
Wang, Zhe
Guo, Jiangtao
Wang, Xiaoqi
Zhu, Huaiqiu
author_sort Zhai, Peng
collection PubMed
description BACKGROUND: During the past decade, the development of high throughput nucleic sequencing and mass spectrometry analysis techniques have enabled the characterization of microbial communities through metagenomics, metatranscriptomics, metaproteomics and metabolomics data. To reveal the diversity of microbial communities and interactions between living conditions and microbes, it is necessary to introduce comparative analysis based upon integration of all four types of data mentioned above. Comparative meta-omics, especially comparative metageomics, has been established as a routine process to highlight the significant differences in taxon composition and functional gene abundance among microbiota samples. Meanwhile, biologists are increasingly concerning about the correlations between meta-omics features and environmental factors, which may further decipher the adaptation strategy of a microbial community. RESULTS: We developed a graphical comprehensive analysis software named MetaComp comprising a series of statistical analysis approaches with visualized results for metagenomics and other meta-omics data comparison. This software is capable to read files generated by a variety of upstream programs. After data loading, analyses such as multivariate statistics, hypothesis testing of two-sample, multi-sample as well as two-group sample and a novel function—regression analysis of environmental factors are offered. Here, regression analysis regards meta-omic features as independent variable and environmental factors as dependent variables. Moreover, MetaComp is capable to automatically choose an appropriate two-group sample test based upon the traits of input abundance profiles. We further evaluate the performance of its choice, and exhibit applications for metagenomics, metaproteomics and metabolomics samples. CONCLUSION: MetaComp, an integrative software capable for applying to all meta-omics data, originally distills the influence of living environment on microbial community by regression analysis. Moreover, since the automatically chosen two-group sample test is verified to be outperformed, MetaComp is friendly to users without adequate statistical training. These improvements are aiming to overcome the new challenges under big data era for all meta-omics data. MetaComp is available at: http://cqb.pku.edu.cn/ZhuLab/MetaComp/ and https://github.com/pzhaipku/MetaComp/. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-017-1849-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-56257842017-10-12 MetaComp: comprehensive analysis software for comparative meta-omics including comparative metagenomics Zhai, Peng Yang, Longshu Guo, Xiao Wang, Zhe Guo, Jiangtao Wang, Xiaoqi Zhu, Huaiqiu BMC Bioinformatics Software BACKGROUND: During the past decade, the development of high throughput nucleic sequencing and mass spectrometry analysis techniques have enabled the characterization of microbial communities through metagenomics, metatranscriptomics, metaproteomics and metabolomics data. To reveal the diversity of microbial communities and interactions between living conditions and microbes, it is necessary to introduce comparative analysis based upon integration of all four types of data mentioned above. Comparative meta-omics, especially comparative metageomics, has been established as a routine process to highlight the significant differences in taxon composition and functional gene abundance among microbiota samples. Meanwhile, biologists are increasingly concerning about the correlations between meta-omics features and environmental factors, which may further decipher the adaptation strategy of a microbial community. RESULTS: We developed a graphical comprehensive analysis software named MetaComp comprising a series of statistical analysis approaches with visualized results for metagenomics and other meta-omics data comparison. This software is capable to read files generated by a variety of upstream programs. After data loading, analyses such as multivariate statistics, hypothesis testing of two-sample, multi-sample as well as two-group sample and a novel function—regression analysis of environmental factors are offered. Here, regression analysis regards meta-omic features as independent variable and environmental factors as dependent variables. Moreover, MetaComp is capable to automatically choose an appropriate two-group sample test based upon the traits of input abundance profiles. We further evaluate the performance of its choice, and exhibit applications for metagenomics, metaproteomics and metabolomics samples. CONCLUSION: MetaComp, an integrative software capable for applying to all meta-omics data, originally distills the influence of living environment on microbial community by regression analysis. Moreover, since the automatically chosen two-group sample test is verified to be outperformed, MetaComp is friendly to users without adequate statistical training. These improvements are aiming to overcome the new challenges under big data era for all meta-omics data. MetaComp is available at: http://cqb.pku.edu.cn/ZhuLab/MetaComp/ and https://github.com/pzhaipku/MetaComp/. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-017-1849-8) contains supplementary material, which is available to authorized users. BioMed Central 2017-10-02 /pmc/articles/PMC5625784/ /pubmed/28969605 http://dx.doi.org/10.1186/s12859-017-1849-8 Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver(http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Software
Zhai, Peng
Yang, Longshu
Guo, Xiao
Wang, Zhe
Guo, Jiangtao
Wang, Xiaoqi
Zhu, Huaiqiu
MetaComp: comprehensive analysis software for comparative meta-omics including comparative metagenomics
title MetaComp: comprehensive analysis software for comparative meta-omics including comparative metagenomics
title_full MetaComp: comprehensive analysis software for comparative meta-omics including comparative metagenomics
title_fullStr MetaComp: comprehensive analysis software for comparative meta-omics including comparative metagenomics
title_full_unstemmed MetaComp: comprehensive analysis software for comparative meta-omics including comparative metagenomics
title_short MetaComp: comprehensive analysis software for comparative meta-omics including comparative metagenomics
title_sort metacomp: comprehensive analysis software for comparative meta-omics including comparative metagenomics
topic Software
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5625784/
https://www.ncbi.nlm.nih.gov/pubmed/28969605
http://dx.doi.org/10.1186/s12859-017-1849-8
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